Published in Ann Genet on January 01, 1984
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A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res (1990) 8.52
Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells. Proc Natl Acad Sci U S A (1997) 5.24
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Interleukin 17, a T-cell-derived cytokine, promotes tumorigenicity of human cervical tumors in nude mice. Cancer Res (1999) 2.23
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High resolution R- and G-banding on the same preparation. Hum Genet (1981) 1.94
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Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion. Nat Genet (1994) 1.91
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NSD3, a new SET domain-containing gene, maps to 8p12 and is amplified in human breast cancer cell lines. Genomics (2001) 1.85
A new member of the ETS family fused to EWS in Ewing tumors. Oncogene (1997) 1.79
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Chromosomal evolution in primates: tentative phylogeny from Microcebus murinus (Prosimian) to man. Hum Genet (1979) 1.75
Anatomical ontologies of mosquitoes and ticks, and their web browsers in VectorBase. Insect Mol Biol (2008) 1.70
Epidemic of AIDS related virus infection among intravenous drug abusers. Br Med J (Clin Res Ed) (1986) 1.68
Targeted agents in metastatic Xp11 translocation/TFE3 gene fusion renal cell carcinoma (RCC): a report from the Juvenile RCC Network. Ann Oncol (2010) 1.65
A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes. Cytogenet Cell Genet (1992) 1.64
Independent factors associated with longevity of prosthetic pulmonary valves and valved conduits. J Thorac Cardiovasc Surg (2000) 1.62
Systematic analysis of 95 reciprocal translocations of autosomes. Hum Genet (1978) 1.59
Mapping of single-copy DNA sequences on human chromosomes by in situ hybridization with biotinylated probes: enhancement of detection sensitivity by intensified-fluorescence digital-imaging microscopy. Proc Natl Acad Sci U S A (1989) 1.59
Selective enhancement of collagenase-mediated cleavage of resident type II collagen in cultured osteoarthritic cartilage and arrest with a synthetic inhibitor that spares collagenase 1 (matrix metalloproteinase 1). Arthritis Rheum (2000) 1.57
Perioperative resuscitation knowledge base. Can J Anaesth (1999) 1.54
Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF. Hum Mutat (2004) 1.52
[Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)]. Ann Genet (1972) 1.50
Mutations in OGG1, a gene involved in the repair of oxidative DNA damage, are found in human lung and kidney tumours. Oncogene (1998) 1.49
Who attends a UK diabetes screening programme? Findings from the ADDITION-Cambridge study. Diabet Med (2010) 1.48
Serovar determination and molecular taxonomic correlation in Mycobacterium avium, Mycobacterium intracellulare, and Mycobacterium scrofulaceum: a cooperative study of the International Working Group on Mycobacterial Taxonomy. Int J Syst Bacteriol (1993) 1.48
Severe defect in proglucagon processing in islet A-cells of prohormone convertase 2 null mice. J Biol Chem (2001) 1.45
Sleep and nutritional deprivation and performance of house officers. J Med Educ (1985) 1.44
[The Dr phenotype: a study of threee cases with a ring D chromosome]. Ann Genet (1968) 1.41
Bilateral renal oncocytosis with renal failure. Arch Pathol Lab Med (2001) 1.41
Spontaneous dissection of native coronary arteries. Heart (2005) 1.41
Survey of chiropractic in Dade County, Florida. J Manipulative Physiol Ther (1982) 1.41
[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)]. Cytogenet Cell Genet (1973) 1.40
Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition. Hum Mol Genet (1997) 1.40
Assessing HER2 gene amplification as a potential target for therapy in invasive urothelial bladder cancer with a standardized methodology: results in 1005 patients. Ann Oncol (2009) 1.40
Tail docking. Vet Rec (1990) 1.40
Chromosomal CGH identifies patients with a higher risk of relapse in neuroblastoma without MYCN amplification. Br J Cancer (2007) 1.39
Effect of waterfowl (Anas platyrhynchos) on indicator bacteria populations in a recreational lake Madison, Wisconsin. Appl Environ Microbiol (1979) 1.38
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8). Nucleic Acids Res (1987) 1.38
Observation of an antimatter hypernucleus. Science (2010) 1.38
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia. Mutat Res (1980) 1.38
Constitutional balanced translocations in patients with solid tumors. Cancer Genet Cytogenet (1992) 1.38
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D). J Med Genet (2014) 1.36
Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment. Chromosoma (1976) 1.36
Type II collagen degradation and its regulation in articular cartilage in osteoarthritis. Ann Rheum Dis (2002) 1.36
[The mechanism of chromosome segmentation induced by BUDR (5-bromodeoxyuridine)]. Ann Genet (1974) 1.35
MLL2, the second human homolog of the Drosophila trithorax gene, maps to 19q13.1 and is amplified in solid tumor cell lines. Oncogene (1999) 1.35
Arrhythmia and survival in patients >18 years of age after the mustard procedure for complete transposition of the great arteries. Am J Cardiol (1999) 1.34
[Mosaic 14 trisomy in a female child with multiple abnormalities]. Ann Genet (1975) 1.34
A nosocomial outbreak of diarrheal disease due to Yersinia enterocolitica serotype 0:5, biotype 1. J Infect Dis (1982) 1.33
Genomic organization of human centromeric alpha satellite DNA: characterization of a chromosome 17 alpha satellite sequence. DNA (1987) 1.33
Sensitivity to CPT-11 of xenografted human colorectal cancers as a function of microsatellite instability and p53 status. Br J Cancer (2000) 1.32
MYC activation associated with the integration of HPV DNA at the MYC locus in genital tumors. Oncogene (2006) 1.31
Detection of DNA amplification in 17 primary breast carcinomas with homogeneously staining regions by a modified comparative genomic hybridization technique. Genes Chromosomes Cancer (1994) 1.30
Which drugs benefit diabetic patients for secondary prevention of myocardial infarction? DARTS/MEMO Collaboration. Diabet Med (1998) 1.29
Report of the American Diabetes Association's Task Force on standardization of the insulin assay. Diabetes (1996) 1.29
Isolation of cDNA clones using yeast artificial chromosome probes. Nucleic Acids Res (1990) 1.28
Trials of corticosteroids to prevent postextubation airway complications. Chest (2001) 1.27
Functional movement test scores improve following a standardized off-season intervention program in professional football players. Scand J Med Sci Sports (2011) 1.26
Physical mapping of human loci homologous to the chicken nov proto-oncogene. Oncogene (1992) 1.26
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients. J Med Genet (2005) 1.26
The right ventricle in congenital heart disease. Heart (2006) 1.24
Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions. Genes Chromosomes Cancer (1995) 1.24
SOD2: a new type of tumor-suppressor gene? Int J Cancer (1992) 1.24
Calibration of immunohistochemistry for assessment of HER2 in breast cancer: results of the French multicentre GEFPICS study. Histopathology (2003) 1.23
Prevalence of cervical pathogens in women with and without inflammatory changes on smear testing. BMJ (1993) 1.23
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]. Humangenetik (1973) 1.23
CD8(+) T-cell autoreactivity to an HLA-B27-restricted self-epitope correlates with ankylosing spondylitis. J Clin Invest (2000) 1.23
Screening with the Alcohol use Disorders Identification Test (AUDIT) in an inner-city population. J Gen Intern Med (1994) 1.23
[New system of chromosome banding: the T bands (author's transl)]. Chromosoma (1973) 1.23
Induction of apoptosis in prostate cancer cell lines by the green tea component, (-)-epigallocatechin-3-gallate. Cancer Lett (1998) 1.22
Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombination. Hum Mol Genet (1992) 1.22
Selective endoreduplication or branched chromosome? Exp Cell Res (1977) 1.22
[Chromosome 8 : complete trisomy and segmental trisomies]. Ann Genet (1977) 1.22
Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses. Genes Chromosomes Cancer (2000) 1.21
Genes occupy a fixed and symmetrical position on sister chromatids. Cell (1991) 1.20
hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities. J Pathol (2007) 1.20
Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3). Genomics (1999) 1.19